Have questions? Visit https://www.reddit.com/r/SNPedia

rs63750695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGTTA;AGTTA) 0 common in clinvar
Make rs63750695(-;-)
Make rs63750695(-;ATTGA)
Make rs63750695(ATTGA;ATTGA)
ReferenceGRCh38 38.1/141
Chromosome7
Position5978675
GenePMS2
is asnp
is mentioned by
dbSNPrs63750695
ebirs63750695
HLIrs63750695
Exacrs63750695
Varsomers63750695
Maprs63750695
PheGenIrs63750695
hapmaprs63750695
1000 genomesrs63750695
hgdprs63750695
ensemblrs63750695
gopubmedrs63750695
geneviewrs63750695
scholarrs63750695
googlers63750695
pharmgkbrs63750695
gwascentralrs63750695
openSNPrs63750695
23andMers63750695
23andMe allrs63750695
SNP Nexus

SNPshotrs63750695
SNPdbers63750695
MSV3drs63750695
GWAS Ctlgrs63750695
Max Magnitude0
ClinVar
Risk rs63750695(;)
Alt rs63750695(;)
Reference rs63750695(AGTTA;AGTTA)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene PMS2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000007.13:g.6018306_6018310delAGTTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076846.3, RCV000163763.1,